Radiation as Immunomodulator: Implications for Dendritic Cell-Based Immunotherapy

被引:40
作者
Roses, Robert E. [1 ]
Datta, Jashodeep [1 ]
Czerniecki, Brian J. [1 ,2 ]
机构
[1] Univ Penn, Dept Surg, Philadelphia, PA 19104 USA
[2] Univ Penn, Rena Rowen Breast Ctr, Philadelphia, PA 19104 USA
关键词
ENHANCES TUMOR RESPONSE; CD8(+) T-CELLS; METASTATIC LUNG-CANCER; TOTAL-BODY IRRADIATION; HEAT-SHOCK PROTEINS; NF-KAPPA-B; IONIZING-RADIATION; IMMUNE-RESPONSE; GAMMA-IRRADIATION; BREAST-CANCER;
D O I
10.1667/RR13495.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The last decade has witnessed significant progress in the field of cancer immunotherapy. This has, in part, been driven by a growing recognition that elements of the innate immune response can be harnessed to induce robust immunity against tumor-associated targets. Nonetheless, as clinically effective immunotherapy for the majority of cancers remains a distant goal, attention has shifted toward multimodality approaches to cancer therapy, sometimes combining novel immunotherapeutics and conventional therapeutics. The traditional view of radiation therapy as immunosuppressive has been challenged, prompting a re-evaluation of its potential as an adjunct to, or even a component of immunotherapy. Radiation therapy may enhance expression of tumor-associated antigens, induce targeting of tumor stroma, diminish regulatory T-cell activity and activate effectors of innate immunity such as dendritic cells through Toll-like receptor (TLR)-dependent mechanisms. Here, we review recent progress in the field of dendritic cell-based immunotherapy, evidence for radiation-induced antitumor immunity and TLR signaling and the results of efforts to rationally integrate radiation into dendritic cell-based immunotherapy strategies. (C) 2014 by Radiation Research Society
引用
收藏
页码:211 / 218
页数:8
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